[A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].

Article

[A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].

Rinsho shinkeigaku = Clinical neurology - 1 Jun 1994

Ohnishi A, Ohnari K, Hashimoto T, Hayasaka K, Yoshimura T, Fukushima Y

Abstract excerpt

A 26-year-old man had complaints of insidiously progressive muscle weakness of the legs, worse in the right leg than in the left. Slight to moderate degrees of asymmetrical muscular atrophy and weakness of the distal lower limb muscles, greater in the right leg than in the left, without fascicula...

Topics

Adult
Aged
Aged, 80 and over
Charcot-Marie-Tooth Disease
Female
Humans
Male
Middle Aged
Mutation
Myelin P0 Protein
Myelin Proteins
Neural Conduction
Sural Nerve

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